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. 2017 Dec 21;7:18015. doi: 10.1038/s41598-017-18237-6

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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DT ablation effectively eliminates DTr expressing newborn dentate granule cells. (a) Timeline depicting the experimental treatment paradigm. (b) Images of Prox1 (blue) and DTr (red) immunostained tissue from healthy-control, SE-control and SE-ablation groups. (c) Higher resolution images of Prox1 and DTr immunostaining in the dentate gyrus showing DTr induction in a small number of reactive astrocytes in the dentate molecular layer (arrows) of a SE-control mouse. (d) Percentage of granule cells that were DTr-positive within each treatment group. (e) Number of Prox1-positive dentate granule cells per dentate section. **p < 0.01, ***p < 0.001, scale bars: 100 µm.